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Lamictal in the Treatment of Post-Herpetic Neuralgia

Lamictal in the Treatment of Post-Herpetic Neuralgia-A Safety, Efficacy,Randomized, Double Blind, Placebo Controlled, Cross-Over Study

Status
Terminated
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00295776
Enrollment
Unknown
Registered
2006-02-24
Start date
2005-02-28
Completion date
Unknown
Last updated
2013-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neuralgia, Postherpetic

Keywords

Inclusion Criteria:Minimum of 4 on the Likert Pain Scale.If currently taking TCA and/or Gabapentin, need to have been on stable dose for minimum of 4 weeks., Exclusion Criteria:, Currently on any antiepilepic drugs (AED), except for Gabapentin., Currently taking opioid or unwilling to washout prior to the study,, Pregnant and lactating,, Have active severe systemic disease,, History of Stevens-Johnson syndrome or TEN,

Brief summary

To assess the efficacy of Lamictal for the treatment of pain and reduction of allodynia in patients with post herpetic neuralgia.

Interventions

DRUGLamictal in the treatment of Post-Herpetic Neuralgia

Sponsors

GlaxoSmithKline
CollaboratorINDUSTRY
George Washington University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years

Inclusion criteria

* All patients will be over the age of 18, * Need to have a diagnosis of Post-Herpetic Neuralgia, * Minimum of 4 on the Likert Pain Scale, * If currently taking TCA and/or Gabapentin, need to have been on stable dose for minimum of 4 weeks

Exclusion criteria

* Currently on any antiepileptic drugs (AED), except for Gabapentin. * Currently taking opioid or unwilling to washout prior to the study, * Pregnant and lactating, * Have active severe systemic disease, * History of Stevens-Johnson syndrome or TEN, * Clinically significant abnormal lab values, * Known drug allergy to Lamictal, * Patients on Fibrates (Tricor and Lopid), * History of major psychiatric disturbance and substance abuse. * Valproate due to increase chances of severe rash, * Lidocaine Patch, * Use of hormonal contraceptives (birth control pills, patch, ring, injection)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026